EP1683496B1

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Info

Publication number: EP1683496B1
Application number: EP06008779A
Authority: EP
Inventors: Steven P. Buysse; Kate R. Lawes; Dale F. Schmaltz; Michael J. Lands; S. Wade Lukianow; Kristin D. Johnson; Gary M. Couture; Lap P. Nguyen
Original assignee: Covidien AG
Current assignee: Covidien AG
Priority date: 2002-06-06
Filing date: 2003-06-03
Publication date: 2008-12-10
Anticipated expiration: 2023-06-03
Also published as: DE60307465T2; EP1665995A1; CA2488435A1; DE60325283D1; EP1513464B1; EP1683496A3; AU2009201795A1; DE60307465D1; EP1683496A2; AU2009201795B2; AU2003245381A1; JP2005538818A; AU2003245381B2; ES2317360T3; EP1513464A1; US20060173452A1; ES2270055T3; WO2004052221A1; JP4461022B2

Description

BACKGROUND

Field of the Invention

This disclosure relates to an electrosurgical instrument for performing laparoscopic surgical procedures, and more particularly to a laparoscopic electrosurgical instrument that is capable of grasping vessels and vascular tissue with sufficient foroe between two bipolar jaws to seal the vessel or vascular tissue.

Background of Related Art

Laparoscopic surgical instruments are used to perform surgical operation without making large incisions in the patient. The laparoscopic instruments are inserted into the patient through a cannula, or port, that has been made with a trocar. Typical sizes for cannulas range from three millimeters to twelve millimeters. Smaller cannulas are usually preferred, and this presents a design challenge to instrument manufacturers who must find ways to make surgical instruments that fit through the cannulas.
Certain surgical procedures require cutting blood vessels or vascular tissue. This sometimes presents a problem for surgeons because it is difficult to suture blood vessels using laparoscopic tools. Very small blood vessels, in the range below two millimeters in diameter, can often be closed using standard electrosurgical techniques. If a larger vessel is severed, it may be necessary for the surgeon to convert the laparoscopic procedure into an open-surgical procedure and thereby abandon the benefits of laparoscopy.
Several joumal articles have disclosed methods for sealing small blood vessels using electrosurgery. An article entitledStudies on Coagulation and the Development of an Automatic Computerized Binolar Coaculator, J. Neurosura.. Volume 75, Jul. 1991, describes a bipolar coagulator which is used to seal small blood vessels. The article states that it was not possible to safely coagulate arteries with a diameter larger than 2 to 2.5 mm. A second article is entitledAutomatically Controlled Bipolar Electrocoagulation-"COA-COMP", Neurosurg. Rev. (1984), pp. 187-190. This article describes a method for terminating electrosurgical power to the vessel so that charring of the vessel walls can be avoided.
It has been recently determined that electrosurgical methods may be able to seal larger vessels using an appropriate electrosurgical power curve, coupled with an instrument capable of applying a large closure force to the vessel walls. It is thought that the process of coagulating small vessels is fundamentally different than electrosurgical vessel sealing. Coagulation is defined as a process of desiccating tissue wherein the tissue cells are ruptured and dried. Vessel sealing is defined as the process of liquefying the collagen in the tissue so that it cross-links and reforms into a fused mass. Thus, coagulation of small vessels is sufficient to permanently close them. Larger vessels need to be sealed to assure permanent closure.
It would be desirable to have a surgical tool capable of applying electrosurgical energy, capable of applying a large closure force to the vessel walls, and also capable of fitting through a cannula. A large closure force between the jaws typically requires a large moment about the pivot for each jaw. This presents a challenge because the first and second pins have a small moment arm with respect to the pivot of each jaw. A large force, coupled with a small moment arm, is undesirable because the large forces may shear the first and second pins. It is also undesirable to increase the moment arm of the first and second pins because the physical size of the yoke might not fit through a cannula.
Several bipolar laparoscopic instruments are known. For example,U.S. Pat. No. 3,938,527 discloses a bipolar laparoscopic instrument for tubal cauterization.U.S. Pat. No. 5,250,047 discloses a bipolar laparoscopic instrument with a replaceable electrode tip assemblv.U.S. Pat. No. 5,445,638 discloses a bipolar coagulation and cutting forceps with first and second conductors extending from the distal end.U.S. Pat. No. 5,391,166 discloses a bipolar endoscopic instrument having a detachable working end.U.S. Pat. No. 5,342,359 discloses a bipolar coagulation device.
The present invention solves the problem of providing a large closure force between the jaws of a laparoscopic bipolar electrosurgical instrument, using a compact design that fits through a cannula, without risking structural failure of the instrument yoke.

SUMMARY OF THE INVENTION

The present disclosure relates to a laparoscopic bipolar electrosurgical instrument for sealing tissue and includes a handle having an elongated tube affixed thereto. The tube includes first and second jaw members attached to a distal end thereof which are movable from a first position for approximating tissue to at least one subsequent position for grasping tissue therebetween. Each of the jaw members includes an electrically conductive sealing surface. The handle has a fixed handle and a handle which is movable relative to the fixed handle to effect movement of the jaw members from the first position to the at least one subsequent position for grasping tissue. The jaw members are connected to a source of electrosurgical energy such that the jaw members are capable of conducting bipolar electrosurgical energy through the tissue held therebetween. A stop is included for maintaining a minimum separation distance between opposing sealing surfaces of at least about 0.03 millimeters and a ratchet is included for mairitaining a dosure force in the range of about 3 kg/cm² to about 16 kg/cm² between opposing sealing surfaces. As can be appreciate, the stop member advantageously creates a minimum separation between electrically conductive opposing sealing surfaces to effect an efficient, consistent and uniform tissue seal.
Advantageously, the stop maintains a minimum separation distance of about 0.03 milimeters to about 0.16 millimeters. The stop may be disposed on at least one of the electrically conductive sealing surfaces, or alternatively, the stop may be located adjacent one of the electrically conductive sealing surfaces. Although it is preferable to locate the stop member on one or both of the electrically conductive opposing sealing autfaoes, it may in some instances be advantageous to locate the stop member adjacent the opposing sealing surfaces.
In one embodiment according to the present disclosure, the first jaw member is connected to the bipolar electrosurgical energy source by a pushrod and the second jaw member is connected to the bipolar electrosurgical source by a conductive tube. As can be appreciated, isolating the jaw members in this manner reduces the likelihood of the instrument short circuiting during activation.
In another embodiment, the ratchet is disposed within the fixed handle and at least one complimentary interlocking mechanical interface is disposed on the movable handle. Preferably, the ratchet and the complimentary interlocking mechanical interface provide at least one interlocking position for maintaining a closure force within the range of about 7 kg/cm² to about 13 kg/cm² between opposing sealing surfaces. Ideally, the closure force is in the range of about 4 kg/cm² to about 6.5 kg/cm². As can be appreciated and as mentioned herein, maintaining the closure force within the above working ranges is a key factor in producing an effective and consistent seal,
In yet another embodiment according the present disclosure, the laparoscopic bipolar electrosurgical instrument includes a handle having an elongated tube affixed thereto with first and second jaw members attached to a distal end thereof which each include electrically conductive sealing surfaces. The jaw members are movable from a first position for approximating tissue to at least one subsequent position for grasping tissue therebetween. The handle has a fixed handle and a handle which is movable relative to the fixed handle to effect movement of the law members from the first position to at least one subsequent position for grasping tissue. Advantageously, the sealing surfaces include a non-stick material for reducing tissue adhesion during the sealing process. The first and second jaw members are coupled to a source of bipolar electrosurgical energy and a stop is disposed on at least one of the electrically conductive sealing surfaces to maintain a minimum separation distance between the opposable seal surfaces during sealing.
A ratchet is disposed on one of the fixed and movable handles and at least one complimentary interlocking mechanical interface is disposed on the other of the fixed and movable handles. Advantageously, the ratchet and the complimentary interlocking mechanical interface include at least one interlocking position which maintains a closure force in the range of about 7 kg/cm² to about 13 kg/cm² between opposable seal surfaces.
In one embodiment, the non-stick material is a coating which is deposited on the opposable sealing surfaces. As can be appreciated, this reduces the likelihood of coagulum build-up and sticking. The non-stick coating may be selected from a group of materials consisting of: nitrides and nickel/chrome alloys. Preferably, the non-stick coating includes one of: TiN; ZrN; TiAIN; CrN; nickel/chrome alloys with a Ni/Cr ratio of approximately 5:1; Inconel 600; Ni200; and Ni201.
In one embodiment according to the present disclosure, the opposable sealing surfaces are manufactured from a non-stick material which is a nickel/chrome alloy. For example, the non-stick material may include nickel/chrome alloys with a Ni/Cr ratio of approximately 5:1, Inconel 600, Ni200 and N1201. it is envisioned that these particular materials are advantageous in providing a superior non-stick surface which reduces coagulum build-up and sticking during activation.
Preferably, at least one of the jaw members, handles and elongated tube includes an insulative material disposed thereon which may advantageously be an insulative coating or an insulative sheath.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a perspective view of a laparoscopic bipolar electrosurgical instrument according to the present disclosure;
FIG. 2 is a perspective view of the distal end and jaws of the instrument inFIG. 1;
FIG. 3 is an exploded view of the distal end shown inFIG. 2;
FIG. 4 is perspective view of the distal end of the instrument with the jaws removed;
FIG. 5 is another perspective ofFIG. 4;
FIG. 6 is a side view of an electrical spring contact; and
FIG. 7 is a front view of the spring contact shown inFIG. 6.

DETAILED DESCRIPTION OF THE INVENTION

A laparoscopic bipolarelectrosurgical instrument 10 is shown inFIG. 1. Theinstrument 10 has aproximal end 11 with ahandle 14 for holding and manipulating theinstrument 10, Adistal end 12 on theinstrument 10 is used for surgical manipulation of tissue. Theinstrument 10 comprises anelongate tube 13 that is sized to tit through a cannula for laparoscopic operations, and in different embodiments may be sized to fit through a five to ten millimeter cannulas.
A portion of thedistal end 12 of theinstrument 10 is shown inFIG. 2. Afirst jaw 15 and asecond jaw 16 are shown in an open position. An angle α is subtended by thejaws 15 and 16. Closing of thejaws 15 and 16 is defined as a reduction of the angle a subtended by thejaws 15 and 16. Similarly, opening of thejaw 15 and 16 is defined as an enlargement of the angle α. The angle α is zero when thejaws 15 and 16 are closed together. The center of rotation for thefirst jaws 15 is at thefirst pivot 41, and the center of rotation for thesecond jaw 16 is at the second pivot 42. Thefirst pivot 41 is located on anouter nose piece 32, and fits in a first pivot hole 43 located on thefirst flange 18. The second pivot 42 is located on aninner nose piece 31, and fits in asecond pivot hole 44 located on thesecond flange 20.
Pieces that comprise thedistal end 12 of theinstrument 10 are shown in an exploded view inFIG. 3. Thefirst jaw 15 and thesecond jaw 16 are shown separated from a yoke 17. Thefirst jaw 15 has afirst flange 18 and afirst slot 19 therewithin. Thesecond jaw 16 has asecond flange 20 and a second slot 21 therewithin. Eachjaw 15 and 16 is preferably formed from a single piece of stainless steel or other electrically conductive material.
Referring again toFIG. 3, the yoke 17 is attached to apushrod 22. The yoke 17 Is preferably formed from an electrically insulative material such as plastic. A first side 23 of the yoke 17 faces thefirst flange 18. Asecond side 24 of the yoke 17 faces thesecond flange 20. When the yoke 17 is positioned between theflanges 18 and 20, the yoke 17 also acts to electrically insulate thefirst jaw 15 from thesecond jaw 16. In this manner, bipolar electrosurgical current can be conducted through tissue grasped by thejaws 15 and 16 without short circuiting between theflanges 18 and 20.
A first pin 25 is located on the first side 23 which movably engages thefirst slot 19. Similarly, asecond pin 26 is located on thesecond side 24 to movably engage the second slot 21. Each pin and slot combination works as a cam-follower mechanical linkage. Motion of thepushrod 22 moves the yoke 17 causingpins 25 and 26 to slide within theirrespective slots 19 and 21. Theslots 19 and 21 are angled with respect to the distal ends of thejaws 15 and 16 such that thelaws 15 and 16 move in an arcuate fashion toward and awav from each other. Thepins 25 and 26 are different from thepivots 41 and 42. Thepins 25 and 26 provide a force against the walls of theslots 19 and 21, creating a moment about thepivots 41 and 42.
Theslots 19 and 21 are arranged such that distal motion of thepushrod 22 causes thejaws 15 and 16 to move together. Distei motion of thepushrod 22 is defined as motion in the direction of thedistal end 12 of theinstrument 10. Once thejaws 15 and 16 are closed together, the present invention holds thejaws 15 and 16 together with a compressive force on thepushrod 22.
One of the advantages of this Invention is that shear forces on thepins 25 and 26 can be offloaded to prevent mechanical failure when large forces are being transmitted to thejaws 15 and 16. Eachslot 19 and 20 has a cul-de-sac 27 and 28, respectively, as shown inFIG. 3. The first cul-de-sac 27 is an enlargement of thefirst slot 19 near its distal end. The second cul-de-sac 28 is an enlargement of the second slot 21 near its distal end. The cam-follower motion of thepins 25 and 26 in theslots 19 and 21 will bring thepins 25 and 26 into their respective cul-de-sac 27 and 28. This position of thepins 25 and 26 leaves a very small moment arm between thepins 25 and 26 and thepivots 41 and 42. The yoke 17 hasshoulders 29 and 30 that can provide a relatively large moment about thepivots 41 and 42 to effect a high closure force between thejaws 15 and 16 without a high shear forces on thepins 25 and 26, as described below.
Once thepins 25 and 26 are in the cul-de-sacs 27 and 28, the force from the yoke is transmitted to theflanges 18 and 20 by afirst shoulder 29 and asecond shoulder 30. Theshoulders 29 and 30 abut the proximal end of theflanges 18 and 20 to cause thejaws 15 and 16 to close together. Thepivots 41 and 42 are preferably made of metal and can withstand relatively high shear forces. In contrast, pins 25 and 26 are preferably made of plastic and will break under relatively high shear forces. Thus, theshoulders 29 and 30 provide a moment about thepivots 41 and 42, thereby avoiding the necessity of applying high shear forces to thepins 25 and 26 wherein the moment arm from thepins 25 and 26 would be small. There is an angle α at which thepins 25 and 26 enter their respective cul-de-sacs 27 and 28 and theshoulders 29 and 30 abut theflanges 18 and 20. The angle α at which the forgoing occurs is preferably around three degrees.
The bipolarelectrosurgical instrument 10 has first and second poles of alternating potential that are conducted along theinstrument 10 and through tissue that is grasped between thejaws 15 and 16. The first pole is conducted from theproximal end 11 toward thedistal end 12 along thepushrod 22. The second pole is conducted from theproximal end 11 toward thedistal end 12 along thetube 13. The outer surface of thetube 13 is preferably coated with an electrically insulative material. There is also preferably an electrically insulative barrier between thepushrod 22 and thetube 13 to prevent short circuits in theinstrument 10.
In the preferred embodiment, the distal end of theinstrument 10 comprises aninner nose piece 31 and anouter nose piece 32, as shown inFIG. 2. Theinner nose piece 31 is electrically connected with thepushrod 22, while the outer nose piece is electrically connected with thetube 13. Theinner nose piece 31 and theouter nose piece 32 capture the yoke 17, along with the first andsecond flanges 18 and 20, as shown inFIG. 2. The yoke 17 moves axially, along an axis defined by thetube 13, in a space between the inner andouter nose pieces 31 and 32. Aspacer stake 33 maintains the separation of thenose pieces 31 and 32 at their distal ends. Thenose pieces 31 and 32 provide lateral support for theflanges 18 and 20 to help ensure that thepins 25 and 26 remain within theslots 18 and 21, respectively.
The preferred embodiment also comprises an inner insulator 34 and an outer insulator 35 for maintaining electrical insulation between the poles. The outer insulator 35 is seated between thetube 13 and theinner nose 31, as shown inFIGS. 2 and4. The inner insulator 34 is seated between thetube 13 and thepushrod 22. In this manner, theouter nose piece 32 can provide electrical continuity between thetube 13 and thesecond jaw 16, while the inner nose piece 34 can provide electrical continuity between thepushrod 22 and thefirst jaw 15. Since thepushrod 22 is slidably mounted within thetube 13. the preferred embodiment has aspring contact 36, as shown inFIGS. 6 and 7, which is mounted on thepushrod 22 to maintain an electrical connection with the inner nose piece 34 during axial motion.
The first andsecond jaws 15 and 16 each haveridges 37 and 38 at their distal ends that preferably nest together. Thejaws 15 and 16 also haveseal surfaces 39 and 40, as shown inFIG. 2. The width of the seal surfaces 39 and 40 is a parameter that affects the quality of the surgical outcome. The closure force between thejaws 15 and 16 varies along the length of the seal surfaces 39 and 40, with the largest force at the distal tip and the smallest force at the proximal end of the seal surfaces 39 and 40. It is known that the amount of pressure exerted on the tissue depends on the surface area of the tissue that is in contact with the seal surfaces. In the one embodiment, the width of each seal surface, e.g., 39, is in the range of about 2 to about 5 millimeters, and preferably 4 millimeters width, while the length of eachseal surface 39 and 40 is preferably in the range of about 10 to 30 millimeters.
It has been found through experimentation that good vessel sealing results are obtained when the closure force in grams divided by the width in millimeters is in the range of about 400 to 650 grams per millimeter of seal surface width. Since the closure force varies with the length of the seal surfaces 39 and 40, it has been found to be advantageous to taper the width of the seal surfaces 39 and 4.0 along their length, with the widest width at the proximal end and the narrowest width at the distal end, For example, If the width of theseal surface 39, 40 is 4 millimeters, the closure force is preferably in the range of about 1600 grams to about 2600 grams This design allows thejaws 15 and 16 to apply a relatively constant closure force per unit width, preferably 525 grams per millimeter width which yields a closure force of 2100 grams for a 4 millimeterwidth seal surface 39, 40.
In one embodiment, thehandle 14 includes a fixed handle 50 having a channel 51 defined therein which slidingly receives amovable handle 52.Movable handle 52 Includes ahandgrip 53 defined therein which allows a user to movehandle 52 relative to fixed handle 50.Movable handle 52 also includes a flange 55 having a series of grooves 62 defined therein which mechanically inter-engage a corresponding ratchet 60 disposed within channel 51. Preferably, the ratchet 60 and groove 62 are dimensioned such that successive ratchet positions will yield pressures within a predetermined working range of about 7 kg/cm² to about 13 kg/cm². In one embodiment, the successive ratchet positions are two millimeters apart.
Experimental results in tissue studies suggest that the magnitude of pressure exerted on the tissue by the seal surfaces 39 and 40 is important in assuring a proper surgical outcome. Tissue pressures within a working range of about 3 kg/cm² to about 16 kg/cm² and, preferably, within a working range of 7 kg/cm² to 13 kg/cm² have been shown to be effective for sealing arteries and vascular bundles. Tissue pressures within the range of about 4 kg/cm² to about 6.5 kg/cm² have proven to be particuiatly effective in sealing arteries and tissue bundles.
A method of making a laparoscopic bipolarelectrosurgical instrument 10 is also herein described. The method comprises the step of forming afirst jaw 15 having afirst flange 18 with afirst slot 19, and asecond jaw 16 having asecond flange 20 with a second slot 21. Thejaws 15 and 16 are preferably formed in a casting process, although it is also possible to machine thejaws 15 and 16 from stock. The casting process may include injecting powdered metal under pressure into a mold, and then applying heat.
Other steps in the method include attaching a yoke 17 to apushrod 22, and electrically insulating thefirst flange 18 from thesecond flange 20 with the yoke 17. The yoke 17 is preferably an injection molded plastic part with features including afirst shoulder 29 and asecond shoulder 30.
During assembly of the distal portion of theinstrument 10, steps in the method include engaging a first pin 25 with thefirst slot 19, and engaging asecond pin 26 with the second slot 21. Theslots 19 and 21 are shaped such that a subtended angle α between the first andsecond jaws 15 and 16 decreases with distal motion of the pushrod 17. Theslots 19 and 20 are formed with cul-de-sacs 27 and 28 positioned to relieve shear stresses on the first andsecond pins 25 and 26 at the subtended angle α approximately where the first andsecond shoulders 29 and 30 engage the first andsecond flanges 18 and 20.
Further steps in the method comprise: surrounding at least a portion of thepushrod 22 with an electricallyconductive tube 13; electrically insulating thetube 13 from thepushrod 22; electrically connecting aninner nose piece 31 to thepushrod 22, and electrically connecting anouter nose piece 32 to thetube 13, wherein theinner nose piece 31 and theouter nose piece 32 capture the yoke 17 along with the first andsecond flanges 18 and 20 to conduct bipolar electrosurgical current to the first andsecond jaws 15 and 16. In the preferred embodiment, there is a step of electrically connecting thepushrod 22 and theinner nose piece 31 with aspring contact 36.
The method of making theinstrument 10, in some embodiments, includes the steps of tapering the width of the seal surfaces 39 and 40 along the length of each of the first andsecond jaws 15 and 16.
An electrically insulative coating 70 may be included to substantially cover theelongated tube 13 to protect the surgeon against electrical arcs. Other parts of the instrument may also be protected by the insulative coating 70. An insulative sheath may also be used to covertube 13 or other components of theinstrument 10, e.g., theproximal end 11, handles 50, 52 and the outer surfaces (non-opposing surfaces) of thejaw members 15, 16,
It is envisioned that the outer surface of thejaw members 15 and 16 may include a nickel-based material, coating, stamping, metal injection molding which is designed to reduce adhesion between the jaw members (or components thereof) with the surrounding tissue during activation and sealing. Moreover, it is also contemplated that other components such as thetube 13 and handles 50, 52 may also be coated with the same or a different "non-stick" material. Preferably, the non-stick materials are of a class of materials that provide a smooth surface to prevent mechanical tooth adhesions.
It is also contemplated that the tissue sealing surfaces 39 and 40 of thejaw members 15 and 16, respectively, may be manufactured from one (or a combination of one or more) of the following "non-stick" materials: nickelchrome, chromium nitride, MedCoat 2000 manufactured by The Electrolizing Corporation of OHIO, Inconel 600 and tin-nickel. For example, high nickel chrome alloys and Ni200, Ni201 (~100% Ni) may be made into electrodes or sealing surfaces by metal injection molding, stamping, machining or any like process.
In addition these materials preferably include an optimal surface energy for eliminating sticking due in part to surface texture and susceptibility to surface breakdown due electrical effects and corrosion in the presence of biologic tissues. It is envisioned that these materials exhibit superior non-stick qualities over stainless steel and should be utilized on the instrument in areas where the exposure to pressure and RF energy can create localized "hot spots" more susceptible to tissue adhesion. As can be appreciated, reducing the amount that the tissue "sticks" during sealing improves the overall efficacy of the instrument.
The tissue sealing surfaces 39 and 40 may also be "coated" with one or more of the above materials to achieve the same result, i.e., a "non-stick surface". For example, Nitride coatings (or one or more of the other above-identified materials) may be deposited as a coating on another base material (metal or nonmetal) using a vapor deposition manufacturing technique.
One particular class of materials disclosed herein has demonstrated superior non-stick properties and, in some instances, superior seal quality. For example, nitride coatings which include, but not are not limited to: TiN, ZrN, TIAIN, and CrN are preferred materials used for non-stick purposes. CrN has been found to be particularly useful for non-stick purposes due to its overall surface properties and performance. Other classes of materials have also been found to reducing overall sticking, For example, high nicket/chrome alloys with a Ni/Cr ratio of approximately 5:1 have been found to significantly reduce sticking in bipolar instrumentation. One particularly useful non-stick material in this class is Inconel 600. Bipolar instrumentation having electrodes made from or coated with NI200, NI201 (~100% Ni) also showed improved non-stick performance over typical bipolar stainless steel electrodes.
It has been found experimentally that local current concentrations can result in an uneven tissue effect, and to reduce the possibility of this outcome, eachseal surface 39 and 40 may include aradiused edge 80, 81. As mentioned above, a taperedseal surface 39 and 40 has been shown to be advantageous in certain embodiments because the taper allows for a relatively constant pressure on the tissue along the length of the seal surfaces 39 and 40. The width of the seal surfaces 39 and 40 may be adjusted to assure that the closure force divided by the width is approximately constant along the length.
In one embodiment, astop 90, made from insulative material, is located in the instrument to maintain a minimum separation of at least about 0.03 millimeters between the seal surfaces 39 and 40, as shown inFIG. 3. Preferably, the stop maintains a minimum separation distance in the range of about 0.03 millimeters to about 0.16 millimeters. Thestop 90 reduces the possibility of short circuits between the seal surfaces 39 and 40. It is envisioned thatstop 90 may be positioned proximate thepivots 41 and 42, proximate thestake 33 or adjacent the opposable seal surfaces 39 and 40.
In another embodiment, theinstrument 10 includes a second oralternative stop 95 which is designed to maintain a minimum separation of at least about 0.03 millimeters between the seal surfaces 39 and 40, as shown inFIG. 2. Preferably, thestop 90 and/or thestop 95 maintains a separation distance within the range of about 0.03 millimeters to about 0.16 millimeters. A plurality ofstops 90 and/or 95 (or various pattems ofstops 90, 95) may also be utilized to accomplish this purpose.
The following numbered paragraphs reveal further aspects of the invention.

Paragraphs

1. A laparoscopic bipolar electrosurgical instrument for sealing tissue, comprising:
- a handle having an elongated tube affixed thereto, the tube including first and second jaw members attached to a distal end thereof, the jaw members being movable from a first position for approximating tissue to at least one subsequent oosttton for crasping tissue therebetween each of the jaw members including an electrically conductive sealing surface, the handle inclucfing a fixed handle and a movable handle, the movable handle being movable relative to the fixed handle to effect movement of the jaw members from the first position to the at least one subsequent position for grasping tissue;
- means for connecting the jaw members to a source of alectrosuipical energy such that the opposable seal surfaces are oapabie of conducting electrosurgical energy through tissue held therebetween;
- a stop for maintaining a minimum separation distance of at least about 0.03 millimeters between opposable searing surfaces; and
- means for maintaining a closure force in the range of about 3 kg/cm² to about 16 kg/cm² between opposable sealing surfaces.
2. A laparoscopic bipolar electrosurgical instrument as in paragraph 1, wherein the connecting means includes:
- a pushrod for connecting the first jaw member to a source of electrosurgical energy; and
- a conductive tube for connecting the second jaw member to the source of electrosurgical energy.
3. A laparoscopic bipolar electrosurgical instrument as in paragraph 1 or 2, wherein the maintaining means includes a ratchet disposed within the fixed handle and at least one complementary interlocking mechanical interface disposed on the movable handle, the ratchet and the complementary interlocking mechanical interface providing at least one interlocking position for maintaining a closure force within the range of about 7 kg/cm² to about 13 kg/cm² between opposable sealing surfaces.
4. A laparoscopic bipolar electrosurgical instrument as in any one of the preceding paragraphs, wherein the closure force is in the range of about 4 kg/cm² to about 6.5 kg/cm².
5. A laparoscopic bipolar electrosurgical instrument as in any one of the preceding paragraphs, wherein the stop is disposed on at least one of the sealing surfaces.
6. A laparoscopic bipolar electrosurgical instrument as in any one of the preceding paragraphs, wherein the stop is disposed adjacent to at least one of the sealing surfaces.
7. A laparoscopic bipolar electrosurgical instrument as in any one of the preceding paragraphs, wherein the stop maintains a minimum separation distance between sealing surfaces in the range of about 0.03 millimeters to about 0.16 millimeters.

Claims

A laparoscopic bipolar electrosurgical instrument (10) for sealing tissue, comprising:
a handle (14) having an elongated tube (13) affixed thereto, the tube (13) including first and second jaw members (15, 16) attached to a distal end (12) thereof, the jaw members (15, 16) being movable from a first position for approximating tissue to at least one subsequent position for grasping tissue therebetween, each of the jaw members (15, 16) including an electrically conductive sealing surface, the handle (14) including a fixed handle (50) and a movable handle (52), the movable handle (52) being movable relative to the fixed handle (50) to effect movement of the jaw members (15, 16) from the first position to the at least one subsequent position for grasping tissue, the opposable sealing surfaces (39, 40) including a non-stick material for reducing tissue adhesion during the sealing process;
means for connecting the jaw members (15, 16) to a source of electrosurgical energy such that the opposable sealing surfaces (39, 40) are capable of conducting electrosurgical energy through tissue held therebetween;characterized by
a stop (90) disposed on one of the opposable sealing surfaces (39, 40) for maintaining a minimum separation distance of at least about 0.03 millimeters between the opposable sealing surfaces (39, 40); and
a ratchet (60) disposed on one of the fixed and movable handles (50, 52) and at least one complementary interlocking mechanical interface (55, 62) disposed on the other of the fixed and movable handles (50, 52) the ratchet (60) and the complementary interlocking mechanical interface (62) providing at least one interlocking position to maintain a closure force in the range of about 3 kg/cm² to about 16 kg/cm² between opposable sealing surface (39, 40).
A laparoscopic bipolar electrosurgical instrument according to claim 1, wherein the non-stick material is a coating which is deposited on the opposable sealing surfaces (39, 40).
A laparoscopic bipolar electrosurgical instrument according to claim 1 or 2, wherein the non-stick coating is selected from a group of materials consisting of: nitrides and nickel/chrome alloys.
A laparoscopic bipolar electrosurgical instrument according to claim 3, wherein the non-stick coating includes at least one of: TiN; ZrN; TiAIN; CrN; nickel/chrome alloys with a Ni/Cr ratio of approximately 5:1; Inconel 600; Ni200; and Ni201.
A laparoscopic bipolar electrosurgical instrument according to claim 1, wherein the opposable sealing surfaces (39, 40) are manufactured from a non-stick material.
A laparoscopic bipolar electrosurgical instrument according to claim 5, wherein the non-stick material is a nickel/chrome alloy.
A laparoscopic bipolar electrosurgical instrument according to claim 6, wherein the non-stick material includes at least one of the nickel/chrome alloys with a Ni/Cr ratio of approximately 5:1, Inconel 600, Ni200 and Ni201.
A laparoscopic bipolar electrosurgical instrument according to any one of the preceding claims, wherein at least one of the jaw members (15, 16), handles (14) and elongated tube (13) includes an insulative material disposed thereon.
A laparoscopic bipolar electrosurgical instrument according to claim 8, wherein the insulative material is an insulative coating.
A bipolar electrosurgical instrument according to claim 8, wherein the insulative material is an insulative sheath.